CZ2004274A3 - Kompozice připravené z chlorovaných polymerů a výrobky vyrobené za použití těchto kompozic - Google Patents
Kompozice připravené z chlorovaných polymerů a výrobky vyrobené za použití těchto kompozic Download PDFInfo
- Publication number
- CZ2004274A3 CZ2004274A3 CZ2004274A CZ2004274A CZ2004274A3 CZ 2004274 A3 CZ2004274 A3 CZ 2004274A3 CZ 2004274 A CZ2004274 A CZ 2004274A CZ 2004274 A CZ2004274 A CZ 2004274A CZ 2004274 A3 CZ2004274 A3 CZ 2004274A3
- Authority
- CZ
- Czechia
- Prior art keywords
- bismuth
- acids
- compositions
- polymer composition
- diesters
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 101
- 229920000642 polymer Polymers 0.000 title claims abstract description 89
- 150000003839 salts Chemical class 0.000 claims abstract description 33
- 150000001735 carboxylic acids Chemical class 0.000 claims abstract description 32
- 229910052797 bismuth Inorganic materials 0.000 claims abstract description 31
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical class [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims abstract description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 22
- 239000002253 acid Substances 0.000 claims abstract description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 14
- 150000007513 acids Chemical class 0.000 claims abstract description 11
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 10
- 125000003277 amino group Chemical group 0.000 claims abstract description 8
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims abstract description 5
- -1 trimellitic acid triesters Chemical class 0.000 claims description 29
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 19
- 150000005690 diesters Chemical class 0.000 claims description 17
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 15
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 11
- XMZKTOZTUVQRBF-UHFFFAOYSA-H dibismuth;propanedioate Chemical compound [Bi+3].[Bi+3].[O-]C(=O)CC([O-])=O.[O-]C(=O)CC([O-])=O.[O-]C(=O)CC([O-])=O XMZKTOZTUVQRBF-UHFFFAOYSA-H 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 6
- ARCGXLSVLAOJQL-UHFFFAOYSA-N anhydrous trimellitic acid Natural products OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 6
- ZDHGGOUPMGSLBR-UHFFFAOYSA-K bis(2-hydroxypropanoyloxy)bismuthanyl 2-hydroxypropanoate Chemical compound [Bi+3].CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O ZDHGGOUPMGSLBR-UHFFFAOYSA-K 0.000 claims description 6
- 150000005691 triesters Chemical class 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 3
- 235000011007 phosphoric acid Nutrition 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- 150000008051 alkyl sulfates Chemical class 0.000 claims 1
- 239000000178 monomer Substances 0.000 description 24
- 239000000779 smoke Substances 0.000 description 22
- 238000012360 testing method Methods 0.000 description 15
- RBXBKNSKYADFNQ-AHUNZLEGSA-H [Bi+3].[Bi+3].[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O Chemical compound [Bi+3].[Bi+3].[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O RBXBKNSKYADFNQ-AHUNZLEGSA-H 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 238000002485 combustion reaction Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 150000001621 bismuth Chemical class 0.000 description 5
- MFBGWESXOIGYSS-UHFFFAOYSA-K bismuth;triformate Chemical compound [Bi+3].[O-]C=O.[O-]C=O.[O-]C=O MFBGWESXOIGYSS-UHFFFAOYSA-K 0.000 description 5
- 239000012760 heat stabilizer Substances 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- KSVSSSGJDHLVOL-UHFFFAOYSA-H dibismuth terephthalate Chemical compound [Bi+3].[Bi+3].[O-]C(=O)c1ccc(cc1)C([O-])=O.[O-]C(=O)c1ccc(cc1)C([O-])=O.[O-]C(=O)c1ccc(cc1)C([O-])=O KSVSSSGJDHLVOL-UHFFFAOYSA-H 0.000 description 4
- 239000003063 flame retardant Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 230000008961 swelling Effects 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical class [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 102000055501 telomere Human genes 0.000 description 3
- 108091035539 telomere Proteins 0.000 description 3
- 210000003411 telomere Anatomy 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Chemical class 0.000 description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- 239000004605 External Lubricant Substances 0.000 description 2
- 239000004610 Internal Lubricant Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical group [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 150000001462 antimony Chemical class 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical class [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- RIBBZUAGJAUAPM-UHFFFAOYSA-K bismuth;prop-2-enoate Chemical compound [Bi+3].[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C RIBBZUAGJAUAPM-UHFFFAOYSA-K 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 230000000711 cancerogenic effect Effects 0.000 description 2
- 150000001734 carboxylic acid salts Chemical class 0.000 description 2
- 231100000315 carcinogenic Toxicity 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- SULICOHAQXOMED-YDXPQRMKSA-H dibismuth;(2r,3r)-2,3-dihydroxybutanedioate Chemical compound [Bi+3].[Bi+3].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O.[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O.[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O SULICOHAQXOMED-YDXPQRMKSA-H 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 229920001567 vinyl ester resin Polymers 0.000 description 2
- QYIGOGBGVKONDY-UHFFFAOYSA-N 1-(2-bromo-5-chlorophenyl)-3-methylpyrazole Chemical compound N1=C(C)C=CN1C1=CC(Cl)=CC=C1Br QYIGOGBGVKONDY-UHFFFAOYSA-N 0.000 description 1
- OMVSWZDEEGIJJI-UHFFFAOYSA-N 2,2,4-Trimethyl-1,3-pentadienol diisobutyrate Chemical compound CC(C)C(=O)OC(C(C)C)C(C)(C)COC(=O)C(C)C OMVSWZDEEGIJJI-UHFFFAOYSA-N 0.000 description 1
- KESQFSZFUCZCEI-UHFFFAOYSA-N 2-(5-nitropyridin-2-yl)oxyethanol Chemical compound OCCOC1=CC=C([N+]([O-])=O)C=N1 KESQFSZFUCZCEI-UHFFFAOYSA-N 0.000 description 1
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical class OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 1
- WSUIRDORMCYOBS-UHFFFAOYSA-N 3-chloro-2-methylprop-2-enoic acid Chemical class ClC=C(C)C(O)=O WSUIRDORMCYOBS-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- RWXJUAKUFLIFHP-UHFFFAOYSA-K OC(C(=O)[O-])(C)C.[Bi+3].OC(C(=O)[O-])(C)C.OC(C(=O)[O-])(C)C Chemical compound OC(C(=O)[O-])(C)C.[Bi+3].OC(C(=O)[O-])(C)C.OC(C(=O)[O-])(C)C RWXJUAKUFLIFHP-UHFFFAOYSA-K 0.000 description 1
- ADGIUZYSNFRMTC-UHFFFAOYSA-K OC(C(=O)[O-])CC.[Bi+3].OC(C(=O)[O-])CC.OC(C(=O)[O-])CC Chemical compound OC(C(=O)[O-])CC.[Bi+3].OC(C(=O)[O-])CC.OC(C(=O)[O-])CC ADGIUZYSNFRMTC-UHFFFAOYSA-K 0.000 description 1
- MHZDNGFWJXEXRU-UHFFFAOYSA-K OC(C(=O)[O-])CCC.[Bi+3].OC(C(=O)[O-])CCC.OC(C(=O)[O-])CCC Chemical compound OC(C(=O)[O-])CCC.[Bi+3].OC(C(=O)[O-])CCC.OC(C(=O)[O-])CCC MHZDNGFWJXEXRU-UHFFFAOYSA-K 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical class [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- HFPRBOJTOWZBMJ-UHFFFAOYSA-K [Bi+3].CCC(C)(O)C([O-])=O.CCC(C)(O)C([O-])=O.CCC(C)(O)C([O-])=O Chemical compound [Bi+3].CCC(C)(O)C([O-])=O.CCC(C)(O)C([O-])=O.CCC(C)(O)C([O-])=O HFPRBOJTOWZBMJ-UHFFFAOYSA-K 0.000 description 1
- NEOBPDGPKKBFDK-UHFFFAOYSA-K [Bi+3].OC1(CC1)C([O-])=O.OC1(CC1)C([O-])=O.OC1(CC1)C([O-])=O Chemical compound [Bi+3].OC1(CC1)C([O-])=O.OC1(CC1)C([O-])=O.OC1(CC1)C([O-])=O NEOBPDGPKKBFDK-UHFFFAOYSA-K 0.000 description 1
- NKQOBHBDMZXBMA-UHFFFAOYSA-H [Bi+3].[Bi+3].[O-]C(=O)C1(CC1)C([O-])=O.[O-]C(=O)C1(CC1)C([O-])=O.[O-]C(=O)C1(CC1)C([O-])=O Chemical compound [Bi+3].[Bi+3].[O-]C(=O)C1(CC1)C([O-])=O.[O-]C(=O)C1(CC1)C([O-])=O.[O-]C(=O)C1(CC1)C([O-])=O NKQOBHBDMZXBMA-UHFFFAOYSA-H 0.000 description 1
- NMLRKAYBZCNQBX-UHFFFAOYSA-H [Bi+3].[Bi+3].[O-]C(=O)CCCCC([O-])=O.[O-]C(=O)CCCCC([O-])=O.[O-]C(=O)CCCCC([O-])=O Chemical compound [Bi+3].[Bi+3].[O-]C(=O)CCCCC([O-])=O.[O-]C(=O)CCCCC([O-])=O.[O-]C(=O)CCCCC([O-])=O NMLRKAYBZCNQBX-UHFFFAOYSA-H 0.000 description 1
- BOKFRKYTRPYRAP-UHFFFAOYSA-H [Bi+3].[Bi+3].[O-]C(=O)CCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCC([O-])=O Chemical compound [Bi+3].[Bi+3].[O-]C(=O)CCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCC([O-])=O BOKFRKYTRPYRAP-UHFFFAOYSA-H 0.000 description 1
- RKDITYORLQEOBC-UHFFFAOYSA-H [Bi+3].[Bi+3].[O-]C(=O)CCCCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCCCC([O-])=O Chemical compound [Bi+3].[Bi+3].[O-]C(=O)CCCCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCCCC([O-])=O RKDITYORLQEOBC-UHFFFAOYSA-H 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical class [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- MVNXWYKGVPTOHV-UHFFFAOYSA-K bis(2,2-dihydroxyhexadecanoyloxy)bismuthanyl 2,2-dihydroxyhexadecanoate Chemical class OC(C(=O)[O-])(CCCCCCCCCCCCCC)O.[Bi+3].OC(C(=O)[O-])(CCCCCCCCCCCCCC)O.OC(C(=O)[O-])(CCCCCCCCCCCCCC)O MVNXWYKGVPTOHV-UHFFFAOYSA-K 0.000 description 1
- JRRZEBYHAIRRQL-UHFFFAOYSA-K bis(2,2-dihydroxyicosanoyloxy)bismuthanyl 2,2-dihydroxyicosanoate Chemical class OC(C(=O)[O-])(CCCCCCCCCCCCCCCCCC)O.[Bi+3].OC(C(=O)[O-])(CCCCCCCCCCCCCCCCCC)O.OC(C(=O)[O-])(CCCCCCCCCCCCCCCCCC)O JRRZEBYHAIRRQL-UHFFFAOYSA-K 0.000 description 1
- QQOQGLYWSWVHAV-UHFFFAOYSA-K bis(2,2-dihydroxyoctadecanoyloxy)bismuthanyl 2,2-dihydroxyoctadecanoate Chemical class OC(C(=O)[O-])(CCCCCCCCCCCCCCCC)O.[Bi+3].OC(C(=O)[O-])(CCCCCCCCCCCCCCCC)O.OC(C(=O)[O-])(CCCCCCCCCCCCCCCC)O QQOQGLYWSWVHAV-UHFFFAOYSA-K 0.000 description 1
- JXABFYOLBMJBDF-UHFFFAOYSA-K bis(2,2-dihydroxytetradecanoyloxy)bismuthanyl 2,2-dihydroxytetradecanoate Chemical class OC(C(=O)[O-])(CCCCCCCCCCCC)O.[Bi+3].OC(C(=O)[O-])(CCCCCCCCCCCC)O.OC(C(=O)[O-])(CCCCCCCCCCCC)O JXABFYOLBMJBDF-UHFFFAOYSA-K 0.000 description 1
- BRFAZONDEJSRAN-UHFFFAOYSA-K bis(2-hydroxyheptanoyloxy)bismuthanyl 2-hydroxyheptanoate Chemical compound OC(C(=O)[O-])CCCCC.[Bi+3].OC(C(=O)[O-])CCCCC.OC(C(=O)[O-])CCCCC BRFAZONDEJSRAN-UHFFFAOYSA-K 0.000 description 1
- OXPYHORLOYRYJT-UHFFFAOYSA-K bis(2-hydroxynonanoyloxy)bismuthanyl 2-hydroxynonanoate Chemical class OC(C(=O)[O-])CCCCCCC.[Bi+3].OC(C(=O)[O-])CCCCCCC.OC(C(=O)[O-])CCCCCCC OXPYHORLOYRYJT-UHFFFAOYSA-K 0.000 description 1
- CWUILNNPTVNJJR-UHFFFAOYSA-K bis(2-hydroxyoctanoyloxy)bismuthanyl 2-hydroxyoctanoate Chemical class OC(C(=O)[O-])CCCCCC.[Bi+3].OC(C(=O)[O-])CCCCCC.OC(C(=O)[O-])CCCCCC CWUILNNPTVNJJR-UHFFFAOYSA-K 0.000 description 1
- KCUWKDXTYNNGAA-UHFFFAOYSA-H bis(4,19-dioxo-1,3-dioxa-2-bismacyclononadec-2-yl) hexadecanedioate Chemical compound [Bi+3].[Bi+3].[O-]C(=O)CCCCCCCCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCCCCCCCC([O-])=O.[O-]C(=O)CCCCCCCCCCCCCCC([O-])=O KCUWKDXTYNNGAA-UHFFFAOYSA-H 0.000 description 1
- SXPRFJXDDZEEHT-UHFFFAOYSA-K bis(4-hydroxybutanoyloxy)bismuthanyl 4-hydroxybutanoate Chemical compound OCCCC(=O)[O-].[Bi+3].OCCCC(=O)[O-].OCCCC(=O)[O-] SXPRFJXDDZEEHT-UHFFFAOYSA-K 0.000 description 1
- NDJPOZBDVOBLOM-UHFFFAOYSA-K bis(5-hydroxypentanoyloxy)bismuthanyl 5-hydroxypentanoate Chemical compound OCCCCC(=O)[O-].[Bi+3].OCCCCC(=O)[O-].OCCCCC(=O)[O-] NDJPOZBDVOBLOM-UHFFFAOYSA-K 0.000 description 1
- RHGQOMYDGHIKFH-GNOQXXQHSA-K bis[[(z)-octadec-9-enoyl]oxy]bismuthanyl (z)-octadec-9-enoate Chemical compound [Bi+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O RHGQOMYDGHIKFH-GNOQXXQHSA-K 0.000 description 1
- UQOQXWZPXFPRBR-UHFFFAOYSA-K bismuth dodecanoate Chemical compound [Bi+3].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O UQOQXWZPXFPRBR-UHFFFAOYSA-K 0.000 description 1
- 229940049676 bismuth hydroxide Drugs 0.000 description 1
- HGSSJXRWSCRNPH-UHFFFAOYSA-K bismuth;butanoate Chemical compound [Bi+3].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O HGSSJXRWSCRNPH-UHFFFAOYSA-K 0.000 description 1
- TZSXPYWRDWEXHG-UHFFFAOYSA-K bismuth;trihydroxide Chemical compound [OH-].[OH-].[OH-].[Bi+3] TZSXPYWRDWEXHG-UHFFFAOYSA-K 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical class [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Chemical class 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000005534 decanoate group Chemical class 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- LBVKKIZHXBASRJ-UHFFFAOYSA-K di(hexadecanoyloxy)bismuthanyl hexadecanoate Chemical compound [Bi+3].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O LBVKKIZHXBASRJ-UHFFFAOYSA-K 0.000 description 1
- GRBFCEINWFRDOG-UHFFFAOYSA-K di(octadecanoyloxy)bismuthanyl octadecanoate Chemical compound [Bi+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O GRBFCEINWFRDOG-UHFFFAOYSA-K 0.000 description 1
- OXQJISYJYOWYJK-UHFFFAOYSA-H dibismuth pentanedioate Chemical compound [Bi+3].[Bi+3].[O-]C(=O)CCCC([O-])=O.[O-]C(=O)CCCC([O-])=O.[O-]C(=O)CCCC([O-])=O OXQJISYJYOWYJK-UHFFFAOYSA-H 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006261 foam material Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- WLJVNTCWHIRURA-UHFFFAOYSA-M pimelate(1-) Chemical compound OC(=O)CCCCCC([O-])=O WLJVNTCWHIRURA-UHFFFAOYSA-M 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0111065A FR2828885B1 (fr) | 2001-08-23 | 2001-08-23 | Compositions de polymeres clores et articles fabriques en utilisant ces compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CZ2004274A3 true CZ2004274A3 (cs) | 2004-07-14 |
Family
ID=8866703
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ2004274A CZ2004274A3 (cs) | 2001-08-23 | 2002-08-21 | Kompozice připravené z chlorovaných polymerů a výrobky vyrobené za použití těchto kompozic |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20040242743A1 (fr) |
| EP (1) | EP1423462A1 (fr) |
| JP (1) | JP2005523343A (fr) |
| KR (1) | KR20040043196A (fr) |
| CN (1) | CN1571813A (fr) |
| AR (1) | AR036280A1 (fr) |
| BR (1) | BR0212082A (fr) |
| CA (1) | CA2457221A1 (fr) |
| CZ (1) | CZ2004274A3 (fr) |
| FR (1) | FR2828885B1 (fr) |
| MX (1) | MXPA04001657A (fr) |
| NO (1) | NO20040753L (fr) |
| PL (1) | PL373660A1 (fr) |
| TW (1) | TW575625B (fr) |
| WO (1) | WO2003018683A1 (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008512544A (ja) * | 2004-12-08 | 2008-04-24 | エルジー・ケム・リミテッド | 塩化ビニル樹脂用加工助剤及びその製造方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR965036A (fr) * | 1947-04-23 | 1950-08-31 | ||
| US4029682A (en) * | 1974-12-23 | 1977-06-14 | Emery Industries, Inc. | Soaps and ester-soaps of α-olefin derived high molecular weight acids |
| US3975359A (en) * | 1974-12-30 | 1976-08-17 | The B. F. Goodrich Company | Smoke retardant vinyl chloride and vinylidene chloride polymer compositions |
| US4279807A (en) * | 1979-01-02 | 1981-07-21 | M&T Chemicals Inc. | Synergistic heat stabilizer compositions containing an antimony or a bismuth compound |
| FR2523989A1 (fr) * | 1982-03-25 | 1983-09-30 | Solvay | Compositions a base de polymeres du chlorure de vinyle presentant une fumigenicite reduite |
-
2001
- 2001-08-23 FR FR0111065A patent/FR2828885B1/fr not_active Expired - Fee Related
-
2002
- 2002-08-15 TW TW91118431A patent/TW575625B/zh active
- 2002-08-21 EP EP02774532A patent/EP1423462A1/fr not_active Withdrawn
- 2002-08-21 CZ CZ2004274A patent/CZ2004274A3/cs unknown
- 2002-08-21 MX MXPA04001657A patent/MXPA04001657A/es unknown
- 2002-08-21 JP JP2003523538A patent/JP2005523343A/ja not_active Abandoned
- 2002-08-21 BR BR0212082-8A patent/BR0212082A/pt not_active IP Right Cessation
- 2002-08-21 PL PL02373660A patent/PL373660A1/xx not_active Application Discontinuation
- 2002-08-21 WO PCT/EP2002/009414 patent/WO2003018683A1/fr not_active Ceased
- 2002-08-21 KR KR10-2004-7002319A patent/KR20040043196A/ko not_active Withdrawn
- 2002-08-21 CA CA002457221A patent/CA2457221A1/fr not_active Abandoned
- 2002-08-21 CN CNA028208145A patent/CN1571813A/zh active Pending
- 2002-08-21 US US10/485,825 patent/US20040242743A1/en not_active Abandoned
- 2002-08-22 AR ARP020103156A patent/AR036280A1/es active IP Right Grant
-
2004
- 2004-02-20 NO NO20040753A patent/NO20040753L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20040753L (no) | 2004-04-22 |
| TW575625B (en) | 2004-02-11 |
| US20040242743A1 (en) | 2004-12-02 |
| FR2828885B1 (fr) | 2003-11-21 |
| NO20040753D0 (no) | 2004-02-20 |
| EP1423462A1 (fr) | 2004-06-02 |
| FR2828885A1 (fr) | 2003-02-28 |
| WO2003018683A1 (fr) | 2003-03-06 |
| CA2457221A1 (fr) | 2003-03-06 |
| PL373660A1 (en) | 2005-09-05 |
| MXPA04001657A (es) | 2004-05-31 |
| BR0212082A (pt) | 2004-09-28 |
| AR036280A1 (es) | 2004-08-25 |
| KR20040043196A (ko) | 2004-05-22 |
| CN1571813A (zh) | 2005-01-26 |
| JP2005523343A (ja) | 2005-08-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7087670B2 (en) | Flame-resistant intumescent mixtures | |
| JP3036405B2 (ja) | 塩化ビニル系樹脂組成物 | |
| EP2241595A1 (fr) | Compositions polymères stabilisées | |
| CN101743279A (zh) | 用作pvc的共稳定剂的羧基改性的聚乙烯醇 | |
| JP5137861B2 (ja) | 塩化ビニル系樹脂組成物 | |
| WO2008018521A1 (fr) | Composition de résine de chlorure de vinyle transparente et de retardement des flammes et produit moulé | |
| CZ2004274A3 (cs) | Kompozice připravené z chlorovaných polymerů a výrobky vyrobené za použití těchto kompozic | |
| PL103567B1 (pl) | Mieszanka plastyfikowanego polihalogenku winylu wytwarzajaca podczas palenia malo dymu | |
| US5350550A (en) | Method of production of a plastic laminate | |
| EP1368422B1 (fr) | Compositions polymeres comprenant des telomeres et des articles ou parties d'articles fabriques a l'aide de ces compositions | |
| US11692091B2 (en) | Resin composition for injection molding | |
| EP2093249A1 (fr) | Composition de PVC non plastifiée | |
| JPS5837039A (ja) | 低発煙性軟質ポリ塩化ビニル組成物 | |
| KR20220112987A (ko) | 친환경 가소제 조성물, 및 이를 포함하는 수지 조성물 | |
| KR102865296B1 (ko) | 가소제 조성물 | |
| JPH10195265A (ja) | 塩化ビニル系樹脂組成物 | |
| JPS62167338A (ja) | 難燃性ポリオレフイン組成物 | |
| JPS5911349A (ja) | 難燃性軟質熱可塑性樹脂組成物 | |
| JPH1180472A (ja) | 塩素系樹脂組成物 | |
| JP7374984B2 (ja) | アイオノマー組成物 | |
| JP2020147694A (ja) | 床材用樹脂組成物および床材 | |
| WO2025197666A1 (fr) | Composition de résine à base de chlorure de vinyle, corps moulé en résine à base de chlorure de vinyle et particules composites | |
| JP2000080229A (ja) | 塩化ビニル系重合体組成物 | |
| CN116745352A (zh) | 增塑剂组合物及包含该增塑剂组合物的氯乙烯树脂组合物 | |
| JPH06145493A (ja) | 塩化ビニル系樹脂用プレートアウト防止剤及び該プレートアウト防止剤を用いる型汚染防止塩化ビニル系樹脂組成物 |